Product Details

SNP ID

rs34465415

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:87828392 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAGAACATATGGAAAAGTGTATTGT[A/G]TGAGTCTGTCTAAAATGATGACAGA

Phenotype

MIM: 605912

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

MEPE PubMed Links

Additional Information

For this assay, SNP(s) [rs144294200] are located under a probe and SNP(s) [rs79407373] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

MEPE

Gene Name

matrix extracellular phosphoglycoprotein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001184694.2		Intron			NP_001171623.1
NM_001184695.1		Intron			NP_001171624.1
NM_001184696.1		Intron			NP_001171625.1
NM_001184697.1		Intron			NP_001171626.1
NM_001291183.1		Intron			NP_001278112.1
NM_020203.3		Intron			NP_064588.1
XM_006714278.2		Intron			XP_006714341.1

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